Published June 11, 2007 | Version v1
Journal article

Purification, crystallization and preliminary crystallographic analysis of Est25: a ketoprofen-specific hormone-sensitive lipase

  • 1. Department of Biological and Molecular Engineering, College of Engineering, Ajou University, Suwon (Korea, Republic of)
  • 2. Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon (Korea, Republic of)

Description

Est25, a ketoprofen-specific hormone-sensitive lipase from a metagenomic library, was crystallized and diffraction data were collected to 1.49 Å resolution. Ketoprofen, a nonsteroidal anti-inflammatory drug, inhibits the synthesis of prostaglandin. A novel hydrolase (Est25) with high ketoprofen specificity has previously been identified using a metagenomic library from environmental samples. Recombinant Est25 protein with a histidine tag at the N-terminus was expressed in Escherichia coli and purified in a homogenous form. Est25 was crystallized from 2.4 M sodium malonate pH 7.0 and X-ray diffraction data were collected to 1.49 Å using synchrotron radiation. The crystals belong to the monoclinic space group C2, with unit-cell parameters a = 197.8, b = 95.2, c = 99.4 Å, β = 97.1°

Availability note (English)

Available from http://dx.doi.org/10.1107/S1744309107026152; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2335126

Additional details

Publishing Information

Journal Title
Acta Crystallographica. Section F
Journal Volume
63
Journal Issue
Pt 7
Journal Page Range
p. 579-581
ISSN
1744-3091
CODEN
ACSFCL

Optional Information

Copyright
Copyright (c) International Union of Crystallography 2007
Notes
PMCID: PMC2335126; PMID: 17620715; PUBLISHER-ID: en5237; OAI: oai:pubmedcentral.nih.gov:2335126